Clinical Research Coordinator

Duties
- Coordinate and oversee clinical research studies from start to finish
- Review and analyze study protocols, informed consent forms, and other study-related documents
- Ensure compliance with FDA regulations, GCP guidelines, and institutional policies
- Recruit and screen potential study participants
- Obtain informed consent from participants and explain study procedures
- Collect and record data accurately and in a timely manner
- Coordinate study visits, including scheduling appointments and arranging necessary tests or procedures
- Perform blood sampling and other clinical procedures as required by the study protocol
- Maintain accurate and organized study documentation
- Supervise and train research staff involved in the study
- Collaborate with investigators, sponsors, and other stakeholders to ensure smooth conduct of the study

Qualifications
- Preferably: Previous experience working as a Clinical Research Coordinator or in a similar role
- Strong knowledge of clinical development processes and FDA regulations
- Familiarity with clinical trials management systems and industry standards
- Proficient in data management and analysis
- Excellent organizational skills with attention to detail
- Ability to work independently and prioritize tasks effectively
- Strong interpersonal and communication skills for effective collaboration with team members, investigators, sponsors, and study participants

Please note that this job description is not exhaustive and additional duties may be assigned as needed.

Pay: $22.00 - $30.00 per hour

Benefits:

• Paid time off

Education:

• Bachelor's (Preferred)

Experience:

• Clinical research: 1 year (Preferred)

Language:

• Spanish (Preferred)

Work Location: In person